Taiwan FDA registration 96ded1ab1c1c934c44e4496363cab6f6

"Probiotic" pylori reagents

TW: "益生" 幽門桿菌試劑
Taiwan flagTaiwan·Risk Class 1·MD BIOTECH CORPORATION·Registered Dec 26, 2005 – Dec 26, 2015Cancelled
Registration details
Analysis ID
96ded1ab1c1c934c44e4496363cab6f6
Customs Code
DHA04400234804
Company information
Manufacturer Country
United States
Authorized Representative
Yisheng Technology Co., Ltd
Product details
Intended Use
Rapid milk coagulation method was used to qualitatively detect antibodies of Spiral pyrenocetii in serum.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.0003 螺旋桿菌屬血清試劑
Import Information
import
Dates and status
Registration Date
Dec 26, 2005
Expiry Date
Dec 26, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Probiotic" pylori reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 96ded1ab1c1c934c44e4496363cab6f6 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Yisheng Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MD BIOTECH CORPORATION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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